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rs539699299

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs539699299(A;A)
Make rs539699299(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position107661725
GeneSLC26A4, SLC26A4-AS1
is asnp
is mentioned by
dbSNPrs539699299
ebirs539699299
HLIrs539699299
Exacrs539699299
Varsomers539699299
Maprs539699299
PheGenIrs539699299
hapmaprs539699299
1000 genomesrs539699299
hgdprs539699299
ensemblrs539699299
gopubmedrs539699299
geneviewrs539699299
scholarrs539699299
googlers539699299
pharmgkbrs539699299
gwascentralrs539699299
openSNPrs539699299
23andMers539699299
23andMe allrs539699299
SNP Nexus

SNPshotrs539699299
SNPdbers539699299
MSV3drs539699299
GWAS Ctlgrs539699299
Max Magnitude0
ClinVar
Risk rs539699299(A;A)
Alt rs539699299(A;A)
Reference rs539699299(C;C)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107302170C>A
CLNSRC
CLNACC RCV000169378.1,